3-Chloro-6-(4-nitrophenyl)pyridazine is an organic compound characterized by its pyridazine core, which is a six-membered aromatic ring containing two nitrogen atoms. The presence of a chlorine atom at the 3-position and a nitrophenyl group at the 6-position contributes to its unique chemical properties. This compound typically exhibits moderate to high stability under standard conditions, but its reactivity can be influenced by the electron-withdrawing nature of the nitro group and the halogen substituent. It may participate in various chemical reactions, including nucleophilic substitutions and electrophilic aromatic substitutions, due to the presence of functional groups that can act as sites for further chemical modification. The compound's solubility can vary depending on the solvent, and it may show biological activity, making it of interest in pharmaceutical research. Safety data should be consulted for handling, as halogenated compounds can pose health risks. Overall, 3-chloro-6-(4-nitrophenyl)pyridazine is a compound of interest in both synthetic organic chemistry and medicinal chemistry.

3-chloro-6-(4-nitrophenyl)pyridazine

99708-47-1: Pyridazine, 3-Chloro-6-(4-Nitrophenyl)-, 3-Chloro-6-(4-nitrophenyl)pyridazine

CAS 99708-47-1: 3-chloro-6-(4-nitrophenyl)pyridazine

3-chloro-6-(4-nitrophenyl)pyridazine

Ref: 10-F522299

3-Chloro-6-(4-nitrophenyl)pyridazine

Ref: 3D-ZDA70847